Variant #0000245434 (NC_000001.10:g.11906068A>G, NM_005957.4:c.-40137T>C (MTHFR))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11906068A>G
DNA change (hg38) g.11846011A>G
Published as NPPA(NM_006172.4):c.454T>C (p.*152Rext*2), NPPA-AS1(NR_037806.1):n.1479+245A>G
ISCN -
DB-ID NPPA_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.13676 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 -/. - c.*5788A>G r.(=) p.(=)
MTHFR NM_005957.4 -/. - c.-40137T>C r.(?) p.(=)
NPPA NM_006172.3 -/. - c.454T>C r.(?) p.(Ter152ArgextTer2)
NPPA-AS1 NR_037806.1 -/. - n.1479+245A>G r.(?) -


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